List of rare mouth diseases
From WikiMD's Food, Medicine & Wellness Encyclopedia
List of Rare Mouth Diseases[edit | edit source]
- 22q11.2 deletion syndrome
- Ablepharon macrostomia syndrome
- Abruzzo-Erickson syndrome
- Acrodysostosis
- Acute necrotizing ulcerative gingivitis
- ADULT syndrome
- Ameloblastic carcinoma
- Amelogenesis imperfecta nephrocalcinosis
- Ankyloblepharon filiforme imperforate anus
- Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome
- Ankylosis of teeth
- Anodontia
- Apert syndrome
- Arthrogryposis multiplex congenita whistling face
- Arthrogryposis, ectodermal dysplasia, cleft lip/palate, and developmental delay
- Atelosteogenesis type 1
- Atelosteogenesis type 2
- Atelosteogenesis type 3
- Auriculo-condylar syndrome
- Ausems Wittebol-Post Hennekam syndrome
- Bamforth syndrome
- Bifid nose
- Bixler Christian Gorlin syndrome
- Branchial arch syndrome X-linked
- Branchiooculofacial syndrome
- Branchiootorenal syndrome
- Bruck syndrome 1
- Cardiomyopathy dilated with woolly hair and keratoderma
- Carey-Fineman-Ziter syndrome
- Catel Manzke syndrome
- CHARGE syndrome
- Charlie M syndrome
- Cherubism
- Childhood hypophosphatasia
- Chitayat Meunier Hodgkinson syndrome
- Classical-like Ehlers-Danlos syndrome
- Cleft hand absent tibia
- Cleft palate short stature vertebral anomalies
- Cleidocranial dysplasia
- Cleidocranial dysplasia recessive form
- Cone-rod dystrophy amelogenesis imperfecta
- Cornelia de Lange syndrome
- Crane-Heise syndrome
- Deafness enamel hypoplasia nail defects
- Deafness oligodontia syndrome
- Dentatorubral-pallidoluysian atrophy
- Dentin dysplasia sclerotic bones
- Dentin dysplasia, coronal
- Dentin dysplasia, type 1
- Dentinogenesis imperfecta
- Dentinogenesis imperfecta type 2
- Dentinogenesis imperfecta type 3
- Dermoodontodysplasia
- Diamond-Blackfan anemia
- Ectodermal dysplasia trichoodontoonychial type
- Ectodermal dysplasia with natal teeth Turnpenny type
- Ectropion inferior cleft lip and or palate
- EEC syndrome
- Femoral facial syndrome
- Fetal hydantoin syndrome
- Fetal indomethacin syndrome
- Fetal methylmercury syndrome
- Fetal minoxidil syndrome
- Fetal valproate syndrome
- Florid cemento-osseous dysplasia
- Fragile X syndrome
- Frontofacionasal dysplasia
- Frontonasal dysplasia
- Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome - See Frontonasal dysplasia
- Frontorhiny - See Frontonasal dysplasia
- Fryns syndrome
- Fuhrmann syndrome
- GAPO syndrome
- Generalized junctional epidermolysis bullosa, non-Herlitz type - See Junctional epidermolysis bullosa
- Genito palato cardiac syndrome
- Gingival fibromatosis with hypertrichosis
- Gingival fibromatosis, 1
- Gingival fibromatosis, 2
- Gingival fibromatosis, 3
- Gingival fibromatosis, 4
- Goldberg-Shprintzen megacolon syndrome
- Goldenhar disease
- Gordon syndrome
- Haim-Munk syndrome
- Hanhart syndrome
- Hardikar syndrome
- Hemi 3 syndrome
- Hemifacial hyperplasia strabismus
- Hemifacial microsomia
- Hemifacial myohyperplasia
- Hyaline fibromatosis syndrome
- Hydrocephalus-cleft palate-joint contractures syndrome
- Hyperthermia induced defects
- Incontinentia pigmenti
- Jones syndrome
- Juberg-Hayward syndrome
- Junctional epidermolysis bullosa generalized intermediate - See Epidermolysis bullosa
- Junctional epidermolysis bullosa, Herlitz type - See Epidermolysis bullosa
- Kabuki syndrome
- Kapur Toriello syndrome
- KBG syndrome
- Kniest dysplasia
- Kohlschutter Tonz syndrome
- Laband syndrome
- Lacrimo-auriculo-dento-digital syndrome
- Lambert syndrome
- Larsen syndrome
- Laryngoonychocutaneous syndrome - See Epidermolysis bullosa
- Late-onset junctional epidermolysis bullosa - See Junctional epidermolysis bullosa
- Late-onset localized junctional epidermolysis bullosa-intellectual disability syndrome
- Localized junctional epidermolysis bullosa, non-Herlitz type - See Junctional epidermolysis bullosa
- Macroglossia
- Macrosomia with lethal microphthalmia
- Malignant hyperthermia arthrogryposis torticollis
- Mandibulofacial dysostosis with microcephaly
- Marden Walker like syndrome
- Marden-Walker syndrome
- Maternal hyperphenylalaninemia
- Maxillonasal dysplasia, Binder type
- Meckel syndrome
- Medeira-Dennis-Donnai syndrome
- Median cleft of upper lip with polyps of facial skin and nasal mucosa
- Mesomelic dwarfism cleft palate camptodactyly
- Methimazole antenatal exposure
- Microbrachycephaly ptosis cleft lip
- Miller syndrome
- Moebius syndrome
- Multiple familial trichoepithelioma 1 - See Multiple familial trichoepithelioma
- Nager acrofacial dysostosis
- Nance-Horan syndrome
- Native American myopathy
- Oculoauriculofrontonasal syndrome
- Oculocerebral syndrome with hypopigmentation
- Oculodentodigital dysplasia
- Oculofaciocardiodental syndrome
- Oculomaxillofacial dysostosis
- Odonto onycho dysplasia with alopecia
- Odontoma dysphagia syndrome
- Odontomicronychial dysplasia
- Odontoonychodermal dysplasia
- Odontotrichomelic syndrome
- Omphalocele cleft palate syndrome lethal
- Oral submucous fibrosis
- Orofaciodigital syndrome 1
- Orofaciodigital syndrome 10
- Orofaciodigital syndrome 11
- Orofaciodigital syndrome 2
- Orofaciodigital syndrome 3
- Orofaciodigital syndrome 4
- Orofaciodigital syndrome 5
- Orofaciodigital syndrome 6
- Orofaciodigital syndrome 8
- Orofaciodigital syndrome 9
- Osteogenesis imperfecta type III
- Osteogenesis imperfecta type IV
- Osteogenesis imperfecta type VI
- Oto-palato-digital syndrome type 1
- Oto-palato-digital syndrome type 2
- Otodental dysplasia
- Pallister W syndrome
- Papillon Lefevre syndrome
- PARC syndrome
- Periodontal Ehlers-Danlos syndrome
- Phenobarbital antenatal exposure
- Pierre Robin sequence
- Pilodental dysplasia with refractive errors
- Pinheiro Freire-Maia Miranda syndrome
- Popliteal pterygium syndrome
- Popliteal pterygium syndrome, Bartsocas-Papas type
- Proteus syndrome
- Proximal chromosome 18q deletion syndrome
- Pyramidal molars-abnormal upper lip syndrome
- Ramon Syndrome
- Rapadilino syndrome
- Richieri Costa Pereira syndrome
- Roberts syndrome
- Rutherfurd syndrome
- Say syndrome
- Schimke immunoosseous dysplasia
- Simpson-Golabi-Behmel syndrome
- Single upper central incisor
- Smith-Lemli-Opitz syndrome
- Smith-Magenis syndrome
- Spondylometaphyseal dysplasia with dentinogenesis imperfecta
- Steatocystoma multiplex with natal teeth
- Stickler syndrome type 1
- Stickler syndrome, type 2
- Stickler syndrome, type 3
- Sturge-Weber syndrome
- Syngnathia cleft palate
- TARP syndrome
- Taurodontia, absent teeth, sparse hair syndrome
- Taurodontism
- Toriello-Carey syndrome
- Townes-Brocks syndrome
- Treacher Collins syndrome
- Tricho-dento-osseous syndrome
- Trichodental syndrome
- Van der Woude syndrome
- Ventricular extrasystoles with syncopal episodes - perodactyly - Robin sequence
- Verloes Bourguignon syndrome
- Verloove Vanhorick Brubakk syndrome
- Waardenburg syndrome type 1
- Waardenburg syndrome type 2
- Waardenburg syndrome type 3
- Warfarin syndrome
- Weissenbacher-Zweymuller syndrome
- Witkop syndrome
- Xanthogranulomatous sialadenitis
- Zlotogora syndrome
NIH genetic and rare disease info[edit source]
List of rare mouth diseases is a rare disease.
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Credits:Most images are courtesy of Wikimedia commons, and templates Wikipedia, licensed under CC BY SA or similar.Contributors: Prab R. Tumpati, MD